Carotid ultrasound versus heart echo to guide fluids in septic shock
Official title: Echocardiographic Left Ventricular End Diastolic Area Versus Carotid Artery Duplex as a Sensitive Indicator for Guiding Fluid Resuscitation in Septic Shock Patients . A Prospective Cohort Study
Run by Ain Shams University · NCT07550400 · Data updated 2026-11-12
This study will test whether carotid artery Doppler flow or left ventricular end-diastolic measurements from echocardiography better predict which adults with septic shock will respond to a fluid bolus.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 50 Years |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Ain Shams University Academic / other |
| Locations | 1 site (Cairo) |
| Status | Recruiting |
| Started | May 3, 2026 |
| Main results expected | November 2, 2026 |
| Study ends | November 12, 2026 |
| Registry record updated | April 24, 2026 |
| Trial ID | NCT07550400 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18–50 with septic shock and signs of acute circulatory failure who can safely undergo carotid and cardiac ultrasound are the ideal candidates.
✕Probably not a fit
Patients with known carotid stenosis >50%, prior carotid surgery, severe valvular heart disease, or local contraindications to carotid Doppler are unlikely to benefit from the carotid-based approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational study enrolling adults with septic shock to compare carotid artery Doppler measurements (VTI and peak velocity) with echocardiographic left ventricular end-diastolic area/volume as predictors of fluid responsiveness. Investigators will obtain baseline carotid and cardiac ultrasound measures, administer a standardized fluid challenge, and repeat measurements to identify changes associated with increased cardiac output (with a ≥15% VTI change indicating responsiveness). The carotid Doppler protocol is presented as a simple, rapid bedside technique that may be easier to learn and perform in critically ill patients than full echocardiography. The work will be conducted at the Faculty of Medicine, Ain Shams University in Cairo and excludes patients with significant carotid stenosis, prior carotid surgery, or severe valvular disease.
Why it matters
Potential benefit: If successful, this could give clinicians a quicker bedside ultrasound method to decide who needs fluids and reduce unnecessary fluid administration.
How similar studies have gone: Prior small studies have shown carotid Doppler VTI can track changes in cardiac output, but direct head-to-head comparisons with LV end-diastolic measures are limited.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria:
* ▪ Age:18-50 years old
* Sex: both males \&females.
* Patients diagnosed with septic shock according to SOFA score more than or equal 1
* Presence of at least one sign of acute circulatory failure from:
1. Low blood pressure (mean arterial pressure \<65 mmHg and / or systolic \<90 mmHg).
2. Tachycardia\> 120 bpm without other obvious cause of circulatory failure.
3. Oliguria \<1 ml / kg during the last hour suggestive of circulatory failure.
4. Blood hyperlactatemia \> 2mmol / l without other obvious cause a systemic circulatory failure.
5. Another sign justifying, for example vascular increase capillary refill time more than 2 seconds.
Exclusion Criteria:
* ▪ Known significant valvular heart disease (sever aortic insufficiency or stenosis)
* Known carotid artery stenosis \>50% or previous carotid surgery
* Clear contraindication to the carotid artery Doppler such as wound or infection or complete or partial occlusion of the carotid artery.
* Arrhythmias affect stroke volume assessment (atrial fibrillation, frequent PVCs)
* Dilated cardiomyopathy.
* Poor transthoracic echocardiographic window
* Patient refusal
Where it's running
-
Faculty of medicine, Ain Shams University
Cairo, Egypt Recruiting
Study contacts
- Study coordinator: baheya kamel
- Email: baheya.hesham.kamel@gmail.com
- Phone: +2-01115746487
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.